This gene encodes one of the six subunits of type IV collagen, the major structural component of basement membranes. Mutations in this gene are associated with X-linked Alport syndrome, also known as hereditary nephritis. Like the other members of the type IV collagen gene family, this gene is organized in a head-to-head conformation with another type IV collagen gene so that each gene pair shares a common promoter. Alternatively spliced transcript variants have been identified for this gene. [provided by RefSeq, Aug 2010]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| COL4A5BA-20-REGO | 20 (40 μL) | 200 μL |
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| COL4A5BA-20-REGR | 20 (40 μL) | 200 μL |
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| COL4A5BA-20-ORGR | 20 (40 μL) | 200 μL |
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| COL4A5BA-20-GOGR | 20 (40 μL) | 200 μL |
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| COL4A5BA-20-GRRE | 20 (40 μL) | 200 μL |
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| COL4A5BA-20-GROR | 20 (40 μL) | 200 μL |
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| COL4A5BA-20-GRGO | 20 (40 μL) | 200 μL |
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| COL4A5BA-20-AQOR | 20 (40 μL) | 200 μL |
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This gene encodes one of the six subunits of type IV collagen, the major structural component of basement membranes. Mutations in this gene are associated with X-linked Alport syndrome, also known as hereditary nephritis. Like the other members of the type IV collagen gene family, this gene is organized in a head-to-head conformation with another type IV collagen gene so that each gene pair shares a common promoter. Alternatively spliced transcript variants have been identified for this gene. [provided by RefSeq, Aug 2010]
Gene Symbol : COL4A5
Gene Name : Collagen type IV alpha 5 chain
Chromosome : CHR X: 108,439,843-108,697,544
Locus : Xq22.3
Alt. Genes : LRPPRC
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